TY - JOUR
T1 - Heterologous Expression of the Biosynthetic Gene Cluster for Verticilactam and Identification of Analogues
AU - Nogawa, Toshihiko
AU - Terai, Atsutaka
AU - Amagai, Keita
AU - Hashimoto, Junko
AU - Futamura, Yushi
AU - Okano, Akiko
AU - Fujie, Manabu
AU - Satoh, Noriyuki
AU - Ikeda, Haruo
AU - Shin-Ya, Kazuo
AU - Osada, Hiroyuki
AU - Takahashi, Shunji
N1 - Funding Information:
We would like to thank Dr. T. Nakamura at RIKEN for the HR-ESITOFMS measurements; Ms. H. Aono at RIKEN for performing the activity tests; and Mr. H. Takagi at RIKEN for technical assistance. We also thank Dr. J. A. V. Lopez for reading the manuscript. The computer calculation using Gaussian 16 was performed using the HOKUSAI at RIKEN. This work was supported in part by the Japan Agency for Medical Research and Development (AMED) and JSPS KAKENHI (grant numbers 17K07784 and 20K05858).
Publisher Copyright:
© 2020 American Chemical Society. All rights reserved.
PY - 2020/12/24
Y1 - 2020/12/24
N2 - Verticilactam and the new geometric isomers, verticilactams B and C, were produced by heterologous expression of the biosynthetic gene cluster for verticilactam using the Streptomyces avermitilis SUKA17 strain. Only verticilactam, a compound with a characteristic β-ketoamide unit within a 16-membered polyketide macrolactam conjugated with an octalin skeleton, had been previously reported having been isolated from Streptomyces spiroverticillatus JC-8444. In this report, minor verticilactam derivatives were isolated from the transformed strain, and their structures elucidated by spectral analysis. Verticilactam B was a geometric isomer at Δ17 and Δ19, and verticilactam C was the Δ19 and Δ21 isomer. In addition, the absolute configuration of verticilactam was confirmed by ECD analysis and NMR chemical shifts. The stereochemistry assignments of the hydroxy groups at C-10 and C-12 were supported by the domain organization of the polyketide synthase identified in the verticilactam gene cluster. Verticilactam showed moderate activity against the malaria parasite Plasmodium falciparum 3D7 strain with no significant cytotoxicity or antimicrobial effects.
AB - Verticilactam and the new geometric isomers, verticilactams B and C, were produced by heterologous expression of the biosynthetic gene cluster for verticilactam using the Streptomyces avermitilis SUKA17 strain. Only verticilactam, a compound with a characteristic β-ketoamide unit within a 16-membered polyketide macrolactam conjugated with an octalin skeleton, had been previously reported having been isolated from Streptomyces spiroverticillatus JC-8444. In this report, minor verticilactam derivatives were isolated from the transformed strain, and their structures elucidated by spectral analysis. Verticilactam B was a geometric isomer at Δ17 and Δ19, and verticilactam C was the Δ19 and Δ21 isomer. In addition, the absolute configuration of verticilactam was confirmed by ECD analysis and NMR chemical shifts. The stereochemistry assignments of the hydroxy groups at C-10 and C-12 were supported by the domain organization of the polyketide synthase identified in the verticilactam gene cluster. Verticilactam showed moderate activity against the malaria parasite Plasmodium falciparum 3D7 strain with no significant cytotoxicity or antimicrobial effects.
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U2 - 10.1021/acs.jnatprod.0c00755
DO - 10.1021/acs.jnatprod.0c00755
M3 - Article
C2 - 33216528
AN - SCOPUS:85097893727
SN - 0163-3864
VL - 83
SP - 3598
EP - 3605
JO - Journal of Natural Products
JF - Journal of Natural Products
IS - 12
ER -